Capital Diamond Star Group
Konglomerat Myanmar melakukan diversifikasi di bidang makanan, farmasi, dan ritel
Capital Diamond Star Group adalah salah satu konglomerat paling dihormati di Myanmar dengan lebih dari 9.000 karyawan di sektor manufaktur makanan, penggilingan tepung, distribusi layanan kesehatan, ritel, jasa keuangan, dan otomotif.
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Yangon, Myanmar
- Founded
- 1960
- Website
- cdsg.com.mm
- Categories
- Mesin Industri, Makanan Khas & Masakan, Perlengkapan Medis & Kesehatan
- Markets
- Myanmar (Burma), Singapura, Thailand
What is established and what is not
No facet of this company has been investigated yet. The facts below are collected records, not an assessment: nothing here confirms manufacturing, ownership or trading status beyond what each record literally says.
Verified facts
- sanctions-clear (green), checked 2026-08-05 - screened by name only: no legal entity is established for this record, so this is not a clearance OpenSanctions
- web-presence-since (green), checked 2026-08-05 Internet Archive (Wayback)
- debarment-clear (green), checked 2026-08-05 - screened by name only: no legal entity is established for this record, so this is not a clearance OpenSanctions
- corporate-mail-on-domain (green), checked 2026-08-05 Mail server of the company domain
Import rules for these goods
- EU imports of food of animal origin and many other food categories must be pre-notified in TRACES and enter through border control posts. European Commission (TRACES)
- US imports require the foreign facility to be FDA-registered and the importer to run a Foreign Supplier Verification Program (FSVP). US FDA
- Medical devices sold in the EU must carry CE marking under the Medical Device Regulation (EU) 2017/745, with a conformity assessment matched to the device risk class. European Commission (MDR)
- For the US market, the maker must have an FDA device establishment registration and product listing; most instruments also need 510(k) premarket clearance. US FDA (devices)